Approvals/TGA/GANCICLOVIR LUPIN ganciclovir (as sodium) 500 mg powder for injection vial

Approved

STANDARD

GANCICLOVIR LUPIN ganciclovir (as sodium) 500 mg powder for injection vial

Southern Cross Pharma Pty Ltd🇦🇺 Therapeutic Goods Administration

Approval Id: 045503719933cd03
Product Name: GANCICLOVIR LUPIN ganciclovir (as sodium) 500 mg powder for injection vial
Artg Id: 280238
Artg Name: GANCICLOVIR LUPIN ganciclovir (as sodium) 500 mg powder for injection vial
Sponsor: Southern Cross Pharma Pty Ltd
Company Detail Path: /organization/southern-cross-pharma-pty-ltd
Artg Date: 2017-08-31
Registration Type: Medicine
Therapeutic Good Type: Medicine
Licence Status: A
Licence Category: RE
Consumer Medicine Info: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-CMI-02343-1
Product Information: http://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent=&id=CP-2024-PI-02372-1

Approved

Agency

TGA

Country

🇦🇺

Approval Date

May 30, 2025

Approval ID

045503719933cd03

Type

Standard